A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569859



Internal ID20942930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41747162..41748744hg38UCSC Ensembl
chr7:41786760..41788342hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381583
hg191583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275940
Samples
Known GenesINHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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